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For: Ocaranza P, Golekoh MC, Andrew SF, Guo MH, Kaplowitz P, Saal H, Rosenfeld RG, Dauber A, Cassorla F, Backeljauw PF, Hwa V. Expanding Genetic and Functional Diagnoses of IGF1R Haploinsufficiencies. Horm Res Paediatr 2017;87:412-22. [PMID: 28395282 DOI: 10.1159/000464143] [Cited by in Crossref: 9] [Cited by in F6Publishing: 14] [Article Influence: 1.8] [Reference Citation Analysis]
Number Citing Articles
1 Kannan S, Bodurtha JN, Hamosh A, Jordan C. Monochorionic twins with 15q26.3 duplication presenting with selective intrauterine growth restriction and discordant cardiac anomalies: A case report. Mol Genet Genomic Med 2022;:e1947. [PMID: 35795918 DOI: 10.1002/mgg3.1947] [Reference Citation Analysis]
2 Singh A, Pajni K, Panigrahi I, Dhoat N, Senapati S, Khetarpal P. Components of IGF-axis in growth disorders: a systematic review and patent landscape report. Endocrine 2022. [PMID: 35523998 DOI: 10.1007/s12020-022-03063-2] [Reference Citation Analysis]
3 Mastromauro C, Chiarelli F; Department of Paediatrics, University of Chieti, Chieti, Italy, Department of Paediatrics, University of Chieti, Chieti, Italy. Novel Insights Into the Genetic Causes of Short Stature in Children. Endocrinology 2022;18:49. [DOI: 10.17925/ee.2022.18.1.49] [Reference Citation Analysis]
4 Fadel IM, Ragab MH, Eid OM, Helmy NA, El-Bassyouni HT, Mazen I. IGF1R, IGFALS, and IGFBP3 gene copy number variations in a group of non-syndromic Egyptian short children. J Genet Eng Biotechnol 2021;19:109. [PMID: 34322776 DOI: 10.1186/s43141-021-00202-6] [Reference Citation Analysis]
5 Shapiro MR, Foster TP, Perry DJ, Rosenfeld RG, Dauber A, McNichols JA, Muir A, Hwa V, Brusko TM, Jacobsen LM. A Novel Mutation in Insulin-Like Growth Factor 1 Receptor (c.641-2A>G) Is Associated with Impaired Growth, Hypoglycemia, and Modified Immune Phenotypes. Horm Res Paediatr 2020;93:322-34. [PMID: 33113547 DOI: 10.1159/000510764] [Reference Citation Analysis]
6 Hwa V, Fujimoto M, Zhu G, Gao W, Foley C, Kumbaji M, Rosenfeld RG. Genetic causes of growth hormone insensitivity beyond GHR. Rev Endocr Metab Disord 2021;22:43-58. [PMID: 33029712 DOI: 10.1007/s11154-020-09603-3] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
7 Gkourogianni A, Andrade AC, Jonsson BA, Segerlund E, Werner-Sperker A, Horemuzova E, Dahlgren J, Burstedt M, Nilsson O. Pre- and postnatal growth failure with microcephaly due to two novel heterozygous IGF1R mutations and response to growth hormone treatment. Acta Paediatr 2020;109:2067-74. [PMID: 32037650 DOI: 10.1111/apa.15218] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
8 Giabicani E, Willems M, Steunou V, Chantot-Bastaraud S, Thibaud N, Abi Habib W, Azzi S, Lam B, Bérard L, Bony-Trifunovic H, Brachet C, Brischoux-Boucher E, Caldagues E, Coutant R, Cuvelier ML, Gelwane G, Guemas I, Houang M, Isidor B, Jeandel C, Lespinasse J, Naud-Saudreau C, Jesuran-Perelroizen M, Perrin L, Piard J, Sechter C, Souchon PF, Storey C, Thomas D, Le Bouc Y, Rossignol S, Netchine I, Brioude F. Increasing knowledge in IGF1R defects: lessons from 35 new patients. J Med Genet 2020;57:160-8. [PMID: 31586944 DOI: 10.1136/jmedgenet-2019-106328] [Cited by in Crossref: 8] [Cited by in F6Publishing: 12] [Article Influence: 2.7] [Reference Citation Analysis]
9 Ocaranza P, Losekoot M, Walenkamp MJE, De Bruin C, Wit JM, Mericq V. Intrauterine Twin Discordancy and Partial Postnatal Catch-up Growth in a Girl with a Pathogenic IGF1R Mutation. J Clin Res Pediatr Endocrinol 2019;11:293-300. [PMID: 30859796 DOI: 10.4274/jcrpe.galenos.2019.2018.0236] [Reference Citation Analysis]
10 Walenkamp MJE, Robers JML, Wit JM, Zandwijken GRJ, van Duyvenvoorde HA, Oostdijk W, Hokken-koelega ACS, Kant SG, Losekoot M. Phenotypic Features and Response to GH Treatment of Patients With a Molecular Defect of the IGF-1 Receptor. The Journal of Clinical Endocrinology & Metabolism 2019;104:3157-71. [DOI: 10.1210/jc.2018-02065] [Cited by in Crossref: 15] [Cited by in F6Publishing: 26] [Article Influence: 5.0] [Reference Citation Analysis]
11 Yang Y, Huang H, Chen K, Yang L, Xie L, Xiong T, Wu X. Novel mutation of type-1 insulin-like growth factor receptor (IGF-1R) gene in a severe short stature pedigree identified by targeted next-generation sequencing. J Genet 2019;98. [DOI: 10.1007/s12041-019-1067-4] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Freire BL, Homma TK, Funari MFA, Lerario AM, Vasques GA, Malaquias AC, Arnhold IJP, Jorge AAL. Multigene Sequencing Analysis of Children Born Small for Gestational Age With Isolated Short Stature. The Journal of Clinical Endocrinology & Metabolism 2019;104:2023-30. [DOI: 10.1210/jc.2018-01971] [Cited by in Crossref: 21] [Cited by in F6Publishing: 29] [Article Influence: 7.0] [Reference Citation Analysis]
13 Domené HM, Fierro-Carrión G. Genetic disorders of GH action pathway. Growth Horm IGF Res 2018;38:19-23. [PMID: 29249625 DOI: 10.1016/j.ghir.2017.12.004] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 2.4] [Reference Citation Analysis]
14 Homma TK, Krepischi ACV, Furuya TK, Honjo RS, Malaquias AC, Bertola DR, Costa SS, Canton AP, Roela RA, Freire BL, Kim CA, Rosenberg C, Jorge AAL. Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown Cause. Horm Res Paediatr 2018;89:13-21. [PMID: 29130988 DOI: 10.1159/000481777] [Cited by in Crossref: 11] [Cited by in F6Publishing: 14] [Article Influence: 2.2] [Reference Citation Analysis]